A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598806



Internal ID6985941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177740464..177745376hg38UCSC Ensembl
Innerchr3:177740479..177745361hg38UCSC Ensembl
Outerchr3:177740449..177745391hg38UCSC Ensembl
chr3:177458252..177463164hg19UCSC Ensembl
Innerchr3:177458267..177463149hg19UCSC Ensembl
Outerchr3:177458237..177463179hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg384913
hg194913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11238187, essv11238186, essv11238188
SamplesHG03619, HG04180, NA20870
Known GenesLINC00578
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598806
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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